1,918 results
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39ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Flat Hand Pad
FDA UDI
Motion Concepts Inc·07540147002718·Flat Hand Pad. (Molded, skinned polyurethane h...
VENTED AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·August 4, 2009
CD HORIZON LEGACY
FDA Adverse Event
Malfunction
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·July 18, 2024
SMART PORT CT
FDA Adverse Event
Injury
·ANGIODYNAMICS, INC·Product code LJT·October 14, 2024
BD PYXIS¿ MEDSTATION¿ ES
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·October 9, 2025
AUTOSUTURE SURGINEEDLE (VERESS NEEDLE)
FDA Adverse Event
Injury
·UNITED STATES SURGICAL CORP·Product code FHP·July 1, 1996
TROCAR NEEDLE
FDA Adverse Event
Malfunction
·COOK MEDICAL·Product code FHP·May 21, 2014
SURGINEEDLE
FDA Adverse Event
Injury
·U.S. SURGICAL CORP.·Product code FHP·January 31, 1995
VARIES NEEDLE
FDA Adverse Event
Malfunction
·STORZ INSTRUMENTS CO.·Product code FHP·October 20, 1994
DEXIDE
FDA Adverse Event
DEXIDE CORP.·Product code FHP·November 22, 1996
ENDOPATH PNEUMOPERITONEUM NEEDLE
FDA Adverse Event
Injury
·LACEY MFG CO.·Product code FHP·November 27, 1996
ENDOPATH
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, INC.·Product code FHP·July 28, 2004
PNEUMO-MATIC INSUFFLATION VERESS NEEDLE
FDA Adverse Event
Malfunction
·COOPER SURGICAL, INC.·Product code FHP·April 2, 2020
STEP VERRES NEEDLE AND TROCAR
FDA Adverse Event
Injury
·INNERDYNE MEDICAL·Product code FHP·May 1, 1995
STEP VERRES NEEDLE AND TROCAR
FDA Adverse Event
Injury
·INNERDYNE MEDICAL·Product code FHP·May 1, 1995
STEP VERRES NEEDLE AND TROCAR
FDA Adverse Event
Injury
·INNERDYNE MEDICAL·Product code FHP·May 1, 1995
STEP VERRES NEEDLE AND TROCAR
FDA Adverse Event
Injury
·INNERDYNE MEDICAL·Product code FHP·May 1, 1995
PNEUMOPERITONEUM NEEDLE 13CM
FDA Adverse Event
Injury
·KARL STORZ·Product code FHP·December 15, 2006
ENDOPATH PNEUMOPERITONEUM NEEDLE
FDA Adverse Event
Malfunction
·LACEY MFG CO.·Product code FHP·January 28, 1997
AUTOSUTURE
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL·Product code FHP·September 29, 2005